Canonical Allele Identifier: CA382910029

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968248T>A (hg19) ; chr11:g.119097538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097538T>A , CM000673.2:g.119097538T>A	GRCh38
NC_000011.9:g.118968248T>A , CM000673.1:g.118968248T>A	GRCh37
NC_000011.8:g.118473458T>A	NCBI36
NG_008918.1:g.9538A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.989A>T
ENST00000524658.2:n.970A>T
ENST00000530052.2:n.1976A>T
ENST00000682191.1:n.1436A>T
ENST00000682192.1:n.1133A>T
ENST00000682232.1:c.*623-241A>T	ENSP00000507302.1:n.*623-241A>T
ENST00000682326.1:c.918-241A>T	ENSP00000508129.1:n.918-241A>T
ENST00000682404.1:n.2032A>T
ENST00000682517.1:n.2335A>T
ENST00000682652.1:n.2205A>T
ENST00000682665.1:n.1631A>T
ENST00000682691.1:n.1631A>T
ENST00000682791.1:c.844A>T	ENSP00000507312.1:p.Thr282Ser
ENST00000682811.1:c.813A>T	ENSP00000508196.1:p.Arg271Ser
ENST00000682883.1:n.1032-241A>T
ENST00000682946.1:c.*13A>T	ENSP00000506856.1:n.*13A>T
ENST00000683143.1:c.*636A>T	ENSP00000507168.1:n.*636A>T
ENST00000683373.1:n.1436A>T
ENST00000683558.1:n.1436A>T
ENST00000683567.1:n.1040A>T
ENST00000683955.1:n.1687A>T
ENST00000684142.1:c.*606A>T	ENSP00000508008.1:n.*606A>T
ENST00000684252.1:n.1328A>T
ENST00000684255.1:c.*636A>T	ENSP00000507398.1:n.*636A>T
ENST00000684315.1:n.1664A>T
ENST00000684345.1:c.*909A>T	ENSP00000507163.1:n.*909A>T
ENST00000684499.1:c.*1036A>T	ENSP00000506800.1:n.*1036A>T
ENST00000684682.1:c.*662A>T	ENSP00000507326.1:n.*662A>T
ENST00000354202.9:c.931A>T MANE Select	ENSP00000346142.4:p.Thr311Ser
ENST00000636404.1:c.233-475A>T
ENST00000638850.1:c.435A>T
ENST00000639704.1:c.838A>T	ENSP00000491336.1:p.Thr280Ser
ENST00000640102.1:c.*584A>T	ENSP00000492027.1:n.*584A>T
ENST00000640747.1:c.*606A>T	ENSP00000492730.1:n.*606A>T
ENST00000354202.8:c.931A>T	ENSP00000346142.4:p.Thr311Ser
ENST00000392834.7:c.*636A>T	ENSP00000376579.3:n.*636A>T
ENST00000409993.6:c.931A>T	ENSP00000386597.2:p.Thr311Ser
ENST00000414373.5:c.*475-241A>T	ENSP00000402019.1:n.*475-241A>T
ENST00000442480.1:c.663A>T	ENSP00000406591.1:p.Arg221Ser
ENST00000461999.1:n.1098A>T
ENST00000481084.5:n.1560A>T
ENST00000524658.1:n.236A>T
ENST00000525456.5:n.745A>T
NM_001382.3:c.931A>T	NP_001373.2:p.Thr311Ser
XM_005271422.2:c.931A>T	XP_005271479.1:p.Thr311Ser
XM_011542648.1:c.610A>T	XP_011540950.1:p.Thr204Ser
XR_947801.1:n.1165-241A>T
XM_005271422.3:c.931A>T	XP_005271479.1:p.Thr311Ser
XM_011542648.2:c.610A>T	XP_011540950.1:p.Thr204Ser
XM_017017293.2:c.610A>T	XP_016872782.1:p.Thr204Ser
XM_017017294.2:c.*13A>T	XP_016872783.1:n.*13A>T
XM_017017295.1:c.415A>T	XP_016872784.1:p.Thr139Ser
XR_001747785.2:n.965A>T
XR_947801.2:n.952-241A>T
NM_001382.4:c.931A>T MANE Select	NP_001373.2:p.Thr311Ser